CH683998A5 - Stabilisatoren für polymere organische Materialien. - Google Patents

Stabilisatoren für polymere organische Materialien. Download PDF

Info

Publication number: CH683998A5
Authority: CH; Switzerland
Prior art keywords: parts; formula; tert; tetrakis; compounds
Prior art date: 1991-07-17

Application number

CH2213/92A

Other languages

German (de)

English (en)

Inventor

Klaus Dr Stoll

Original Assignee

Sandoz Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1991-07-17

Filing date

1992-07-14

Publication date

1994-06-30

1991-07-17 Priority claimed from GB919115380A external-priority patent/GB9115380D0/en

1991-10-15 Priority claimed from GB919121882A external-priority patent/GB9121882D0/en

1992-07-14 Application filed by Sandoz Ag filed Critical Sandoz Ag

1994-06-30 Publication of CH683998A5 publication Critical patent/CH683998A5/de

Links

239000003381 stabilizer Substances 0.000 title claims description 34
239000011368 organic material Substances 0.000 title claims description 5
150000001875 compounds Chemical class 0.000 claims description 20
229910052739 hydrogen Inorganic materials 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical class OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 9
NSOXQYCFHDMMGV-UHFFFAOYSA-N Tetrakis(2-hydroxypropyl)ethylenediamine Chemical compound CC(O)CN(CC(C)O)CCN(CC(C)O)CC(C)O NSOXQYCFHDMMGV-UHFFFAOYSA-N 0.000 claims description 7
229910052698 phosphorus Inorganic materials 0.000 claims description 6
RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 claims description 4
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 4
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
125000002723 alicyclic group Chemical group 0.000 claims description 4
125000001931 aliphatic group Chemical group 0.000 claims description 4
NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 claims description 4
239000011574 phosphorus Substances 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000000463 material Substances 0.000 claims description 3
239000007983 Tris buffer Substances 0.000 claims description 2
125000004437 phosphorous atom Chemical group 0.000 claims description 2
ICKWICRCANNIBI-UHFFFAOYSA-N 2,4-di-tert-butylphenol Chemical compound CC(C)(C)C1=CC=C(O)C(C(C)(C)C)=C1 ICKWICRCANNIBI-UHFFFAOYSA-N 0.000 claims 1
UELGRCOBOPRCQU-UHFFFAOYSA-N biphenylene;hydroxyphosphanyloxyphosphinous acid Chemical compound OPOPO.C1=CC=C2C3=CC=CC=C3C2=C1 UELGRCOBOPRCQU-UHFFFAOYSA-N 0.000 claims 1
PYLSRPMNAYHKLZ-UHFFFAOYSA-N biphenylene;phosphorous acid Chemical compound OP(O)O.C1=CC=C2C3=CC=CC=C3C2=C1 PYLSRPMNAYHKLZ-UHFFFAOYSA-N 0.000 claims 1
239000000470 constituent Substances 0.000 claims 1
239000004753 textile Substances 0.000 claims 1
-1 polyethylene Polymers 0.000 description 38
239000000203 mixture Substances 0.000 description 37
230000007062 hydrolysis Effects 0.000 description 17
238000006460 hydrolysis reaction Methods 0.000 description 17
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 16
238000001125 extrusion Methods 0.000 description 15
229910052757 nitrogen Inorganic materials 0.000 description 14
229920000642 polymer Polymers 0.000 description 11
239000000126 substance Substances 0.000 description 11
230000001681 protective effect Effects 0.000 description 10
229910019142 PO4 Inorganic materials 0.000 description 9
239000003054 catalyst Substances 0.000 description 9
235000021317 phosphate Nutrition 0.000 description 9
150000003254 radicals Chemical class 0.000 description 9
KLLLJCACIRKBDT-UHFFFAOYSA-N 2-phenyl-1H-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=C1 KLLLJCACIRKBDT-UHFFFAOYSA-N 0.000 description 8
150000002431 hydrogen Chemical group 0.000 description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 7
239000005977 Ethylene Substances 0.000 description 7
239000004698 Polyethylene Substances 0.000 description 7
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 7
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 7
239000010452 phosphate Substances 0.000 description 7
229920000573 polyethylene Polymers 0.000 description 7
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
229920001577 copolymer Polymers 0.000 description 5
230000000694 effects Effects 0.000 description 5
229920003023 plastic Polymers 0.000 description 5
239000004033 plastic Substances 0.000 description 5
229920000098 polyolefin Polymers 0.000 description 5
229920005989 resin Polymers 0.000 description 5
239000011347 resin Substances 0.000 description 5
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 4
239000004593 Epoxy Substances 0.000 description 4
239000004743 Polypropylene Substances 0.000 description 4
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
229920002678 cellulose Polymers 0.000 description 4
239000001913 cellulose Substances 0.000 description 4
230000006378 damage Effects 0.000 description 4
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
229920001155 polypropylene Polymers 0.000 description 4
238000003860 storage Methods 0.000 description 4
CWKVFRNCODQPDB-UHFFFAOYSA-N 1-(2-aminoethylamino)propan-2-ol Chemical compound CC(O)CNCCN CWKVFRNCODQPDB-UHFFFAOYSA-N 0.000 description 3
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 3
229920000877 Melamine resin Polymers 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
241000350481 Pterogyne nitens Species 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
229910052782 aluminium Inorganic materials 0.000 description 3
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 3
238000000034 method Methods 0.000 description 3
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
239000004709 Chlorinated polyethylene Substances 0.000 description 2
238000005727 Friedel-Crafts reaction Methods 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
229920002367 Polyisobutene Polymers 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
BEIOEBMXPVYLRY-UHFFFAOYSA-N [4-[4-bis(2,4-ditert-butylphenoxy)phosphanylphenyl]phenyl]-bis(2,4-ditert-butylphenoxy)phosphane Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(C=1C=CC(=CC=1)C=1C=CC(=CC=1)P(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C BEIOEBMXPVYLRY-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
235000013877 carbamide Nutrition 0.000 description 2
239000005018 casein Substances 0.000 description 2
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
235000021240 caseins Nutrition 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000000354 decomposition reaction Methods 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
239000012535 impurity Substances 0.000 description 2
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 2
SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
238000012360 testing method Methods 0.000 description 2
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
HJIAMFHSAAEUKR-UHFFFAOYSA-N (2-hydroxyphenyl)-phenylmethanone Chemical class OC1=CC=CC=C1C(=O)C1=CC=CC=C1 HJIAMFHSAAEUKR-UHFFFAOYSA-N 0.000 description 1
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-Tetramethylpiperidine Substances CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 1
FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical class OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
OUVMWIKEEGQNFZ-UHFFFAOYSA-N 2-hydroxybenzoic acid;[3-(2-hydroxybenzoyl)phenyl]-(2-hydroxyphenyl)methanone Chemical class OC(=O)C1=CC=CC=C1O.OC1=CC=CC=C1C(=O)C1=CC=CC(C(=O)C=2C(=CC=CC=2)O)=C1 OUVMWIKEEGQNFZ-UHFFFAOYSA-N 0.000 description 1
KPYCVQASEGGKEG-UHFFFAOYSA-N 3-hydroxyoxolane-2,5-dione Chemical compound OC1CC(=O)OC1=O KPYCVQASEGGKEG-UHFFFAOYSA-N 0.000 description 1
229960000549 4-dimethylaminophenol Drugs 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
DQEFEBPAPFSJLV-UHFFFAOYSA-N Cellulose propionate Chemical compound CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 DQEFEBPAPFSJLV-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
239000004801 Chlorinated PVC Substances 0.000 description 1
239000004641 Diallyl-phthalate Substances 0.000 description 1
IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
SIHACQYMTNINSJ-UHFFFAOYSA-N P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C1=C(C=2C3=CC=CC=C3C2C=C1)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C Chemical compound P(O)(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C1=C(C=2C3=CC=CC=C3C2C=C1)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C SIHACQYMTNINSJ-UHFFFAOYSA-N 0.000 description 1
239000002033 PVDF binder Substances 0.000 description 1
239000004813 Perfluoroalkoxy alkane Substances 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
239000004697 Polyetherimide Substances 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
229920000265 Polyparaphenylene Polymers 0.000 description 1
229920000491 Polyphenylsulfone Polymers 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
229920001328 Polyvinylidene chloride Polymers 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
239000012963 UV stabilizer Substances 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
239000002253 acid Substances 0.000 description 1
238000005903 acid hydrolysis reaction Methods 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
125000005396 acrylic acid ester group Chemical group 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000032683 aging Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
239000002216 antistatic agent Substances 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
239000003139 biocide Substances 0.000 description 1
QUDWYFHPNIMBFC-UHFFFAOYSA-N bis(prop-2-enyl) benzene-1,2-dicarboxylate Chemical compound C=CCOC(=O)C1=CC=CC=C1C(=O)OCC=C QUDWYFHPNIMBFC-UHFFFAOYSA-N 0.000 description 1
MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
229920006217 cellulose acetate butyrate Polymers 0.000 description 1
229920006218 cellulose propionate Polymers 0.000 description 1
239000012461 cellulose resin Substances 0.000 description 1
229920000457 chlorinated polyvinyl chloride Polymers 0.000 description 1
150000001851 cinnamic acid derivatives Chemical class 0.000 description 1
230000006835 compression Effects 0.000 description 1
238000007906 compression Methods 0.000 description 1
229940118056 cresol / formaldehyde Drugs 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
VRXKSZJBXBVTQW-UHFFFAOYSA-N dihydroxyphosphanyl dihydrogen phosphite 1,2,3,4-tetrakis(2,4-ditert-butylphenyl)biphenylene Chemical compound OP(O)OP(O)O.C(C)(C)(C)C1=C(C=CC(=C1)C(C)(C)C)C1=C(C(=C(C=2C3=CC=CC=C3C12)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C)C1=C(C=C(C=C1)C(C)(C)C)C(C)(C)C VRXKSZJBXBVTQW-UHFFFAOYSA-N 0.000 description 1
CGPRUXZTHGTMKW-UHFFFAOYSA-N ethene;ethyl prop-2-enoate Chemical compound C=C.CCOC(=O)C=C CGPRUXZTHGTMKW-UHFFFAOYSA-N 0.000 description 1
HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000010096 film blowing Methods 0.000 description 1
239000003063 flame retardant Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
HDNHWROHHSBKJG-UHFFFAOYSA-N formaldehyde;furan-2-ylmethanol Chemical compound O=C.OCC1=CC=CO1 HDNHWROHHSBKJG-UHFFFAOYSA-N 0.000 description 1
SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
239000007849 furan resin Substances 0.000 description 1
239000007863 gel particle Substances 0.000 description 1
HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
238000004128 high performance liquid chromatography Methods 0.000 description 1
230000003301 hydrolyzing effect Effects 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004611 light stabiliser Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
238000002074 melt spinning Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000006078 metal deactivator Substances 0.000 description 1
239000002923 metal particle Substances 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
239000012768 molten material Substances 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
229940065472 octyl acrylate Drugs 0.000 description 1
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
239000002530 phenolic antioxidant Substances 0.000 description 1
229920001568 phenolic resin Polymers 0.000 description 1
239000005011 phenolic resin Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
239000002574 poison Substances 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
229920001485 poly(butyl acrylate) polymer Polymers 0.000 description 1
229920002493 poly(chlorotrifluoroethylene) Polymers 0.000 description 1
229920001608 poly(methyl styrenes) Polymers 0.000 description 1
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 1
229920002401 polyacrylamide Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920001707 polybutylene terephthalate Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920002530 polyetherether ketone Polymers 0.000 description 1
229920001601 polyetherimide Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920001228 polyisocyanate Polymers 0.000 description 1
239000005056 polyisocyanate Substances 0.000 description 1
229920002959 polymer blend Polymers 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
229920000193 polymethacrylate Polymers 0.000 description 1
229920001955 polyphenylene ether Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920001343 polytetrafluoroethylene Polymers 0.000 description 1
239000004810 polytetrafluoroethylene Substances 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
229940068984 polyvinyl alcohol Drugs 0.000 description 1
235000019422 polyvinyl alcohol Nutrition 0.000 description 1
229920002620 polyvinyl fluoride Polymers 0.000 description 1
239000005033 polyvinylidene chloride Substances 0.000 description 1
229920002981 polyvinylidene fluoride Polymers 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003336 secondary aromatic amines Chemical class 0.000 description 1
229920005573 silicon-containing polymer Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229910052717 sulfur Chemical group 0.000 description 1
239000011593 sulfur Chemical group 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
229920006305 unsaturated polyester Polymers 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000004383 yellowing Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/17—Amines; Quaternary ammonium compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/53—Phosphorus bound to oxygen bound to oxygen and to carbon only
- C08K5/5393—Phosphonous compounds, e.g. R—P(OR')2

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)

CH2213/92A 1991-07-17 1992-07-14 Stabilisatoren für polymere organische Materialien. CH683998A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB919115380A GB9115380D0 (en)	1991-07-17	1991-07-17	Improvements in or relating to organic compounds
GB919121882A GB9121882D0 (en)	1991-10-15	1991-10-15	Improvements in or relating to organic compounds

Publications (1)

Publication Number	Publication Date
CH683998A5 true CH683998A5 (de)	1994-06-30

Family

ID=26299249

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH2213/92A CH683998A5 (de)	1991-07-17	1992-07-14	Stabilisatoren für polymere organische Materialien.

Country Status (6)

Country	Link
JP (1)	JPH05230282A (it)
CH (1)	CH683998A5 (it)
DE (1)	DE4222648A1 (it)
FR (1)	FR2679913A1 (it)
GB (1)	GB2257706A (it)
IT (1)	IT1297199B1 (it)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB2263280B (en) *	1992-01-17	1996-07-31	Sandoz Ltd	Use of a phosphonite and optionally a phosphite for clarifying propylene polymers
GB2283490A (en) *	1993-11-03	1995-05-10	Sandoz Ltd	Processing stabilizers for polymers
US5468895A (en) *	1994-10-19	1995-11-21	General Electric Company	Amine stabilized amorphous phosphite
DE19501212A1 (de) *	1994-12-22	1996-06-27	Richter Elk Prof Dr Ing	Verfahren zum Herstellen von Bitumen und Asphalt
DE102004022963A1 (de) *	2004-05-10	2005-12-08	Ems-Chemie Ag	Thermoplastische Polyamid-Formmassen
DE102019200596A1 (de) *	2019-01-17	2020-07-23	Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V.	Verwendung einer additivzusammensetzung zum kontrollierten beschleunigten abbau von kondensationspolymeren

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS6155112A (ja) *	1984-08-24	1986-03-19	Ito Seiyu Kk	二液常温硬化型ポリウレタン樹脂組成物
GB8901517D0 (en) *	1989-01-24	1989-03-15	Sandoz Ltd	Improvements in or relating to organic compounds

1992
- 1992-07-10 FR FR9208701A patent/FR2679913A1/fr active Pending
- 1992-07-10 DE DE4222648A patent/DE4222648A1/de not_active Withdrawn
- 1992-07-13 GB GB9214815A patent/GB2257706A/en not_active Withdrawn
- 1992-07-14 CH CH2213/92A patent/CH683998A5/de not_active IP Right Cessation
- 1992-07-14 IT IT92RM000536A patent/IT1297199B1/it active IP Right Grant
- 1992-07-16 JP JP4189633A patent/JPH05230282A/ja active Pending

Also Published As

Publication number	Publication date
FR2679913A1 (fr)	1993-02-05
ITRM920536A1 (it)	1994-01-14
ITRM920536A0 (it)	1992-07-14
GB9214815D0 (en)	1992-08-26
IT1297199B1 (it)	1999-08-03
DE4222648A1 (de)	1993-02-11
JPH05230282A (ja)	1993-09-07
GB2257706A (en)	1993-01-20

Legal Events

Date	Code	Title	Description
1995-03-31	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
EP0002821B1 (de)	1982-06-23	Cyclische Phosphite und mit deren Hilfe stabilisiertes organisches Material
US5364895A (en)	1994-11-15	Hydrolytically stable pentaerythritol diphosphites
DE10309385B4 (de)	2007-01-18	Flammschutzmittel-Stabilisator-Kombination für thermoplastische Polymere und ihre Verwendung sowie flammfest ausgerüstete Kunststoff-Formmassen
KR100452653B1 (ko)	2005-01-17	아민옥사이드안정화제조성물을함유한중합체조성물
CN102712785B (zh)	2014-05-14	具有低凝胶含量和增强的气体褪色性的聚合物
JP2594105B2 (ja)	1997-03-26	有機重合体組成物及びその光劣化に対する安定化方法
DE4001397A1 (de)	1990-07-26	Stabilisatoren fuer polymere materialien
KR100367275B1 (ko)	2003-04-23	포스파이트를 포함하는 중합체 조성물
DE3689577T2 (de)	1994-07-21	Wärmebeständige Polyolefinzusammensetzung.
BRPI0713256B1 (pt)	2018-11-21	composição contendo uma mistura de pelo menos dois fosfitos diferentes de estrutura, composição estabilizada contendo a mesma, artigo de fabricação, método para estabilização de uma resina termoplástica ou elastômero e método para sintetização de uma mistura líquida de pelo menos dois fosfitos líquidos
US20110039996A1 (en)	2011-02-17	Process for Stabilization of Polymer Compositions
DE4418080A1 (de)	1994-12-01	Stabilisatoren für polymere Materialien
DE69418387T2 (de)	1999-12-30	Neo-Diol Phosphite als Polymer-Stabilisatoren
DE69001495T2 (de)	1993-12-09	Dioxaphosphorin-Verbindungen und damit stabilisierte Polyolefin-Zusammensetzungen.
CH683998A5 (de)	1994-06-30	Stabilisatoren für polymere organische Materialien.
US3322718A (en)	1967-05-30	Polyolefins stabilized with phosphites, phenols, and benzotriazoles
DE4233973A1 (de)	1993-04-15	Stabilisatoren fuer polymere verbindungen
DE60209829T2 (de)	2006-11-23	Degradierungsverzögerer für Harzmateriale, chlorierte wasserbeständige Harzzusammensetzung und Methode zur Verzögerung der Degradierung
US5342869A (en)	1994-08-30	Stabilized polymeric compositions
EP0628595B1 (en)	2000-08-23	Organic phosphite ester compositions containing hindered piperidinyl light stabilizers
US20040249030A1 (en)	2004-12-09	Polymer compositions containing stabilizer compounds comprising tricyclodecylmethyl groups
GB2247241A (en)	1992-02-26	Stabilising composition for filled polymeric materials
EP0680486B1 (en)	1999-03-24	Hydrolytically stable pentaerythritol diphosphites
EP0324106B1 (de)	1994-08-10	Verwendung einer Polyolefinformmasse für Dauerkontakt mit extrahierenden Medien
JPS5930842A (ja)	1984-02-18	安定化ポリオレフイン樹脂組成物